HuGE Literature Finder
Records 1-4
Pattern of somatic mutations in patients with Waldenström macroglobulinemia or IgM monoclonal gammopathy of undetermined significance.
Haematologica 2017 Oct . Varettoni Marzia, Zibellini Silvia, Defrancesco Irene, Ferretti Virginia Valeria, Rizzo Ettore, Malcovati Luca, Gallì Anna, Della Porta Matteo Giovanni, Boveri Emanuela, Arcaini Luca, Candido Chiara, Paulli Marco, Cazzola Mar |
Detection of MYD88 L265P and WHIM-like CXCR4 mutation in patients with IgM monoclonal gammopathy related disease.
Annals of hematology 2017 Mar . Cao Xin-Xin, Meng Qi, Cai Hao, He Tian-Hua, Zhang Cong-Li, Su Wei, Sun Jian, Li Yue, Xu Wei, Zhou Dao-Bin, Li Ji |
Somatic mutations in MYD88 and CXCR4 are determinants of clinical presentation and overall survival in Waldenstrom macroglobulinemia.
Blood 2014 May 123 (18): 2791-6. Treon Steven P, Cao Yang, Xu Lian, Yang Guang, Liu Xia, Hunter Zachary |
SDF1/CXCL12 (-801GA) polymorphism is a prognostic factor after treatment initiation in Waldenstrom macroglobulinemia.
Leukemia research 2009 Sep 33 (9): 1204-7. Poulain Stéphanie, Ertault Marjan, Leleu Xavier, Coiteux Valérie, Fernandes José, Stalnikiewicz Laure, Duthilleul Patrick, Morel Pier |
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